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Intra-examiner reproducibility of probing pocket depth using four types of manual periodontal probes, in vivo

Intra-examiner reproducibility of probing pocket depth with four manual probes types in healthy volunteers.

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12611000129987
Enrollment
20
Registered
2011-02-04
Start date
2008-06-01
Completion date
Unknown
Last updated
2020-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

The periodontal probe remains as the best clinical diagnostic tool to collect information regarding the health status and the attachment level of periodontal tissues. The aim of the present study is to evaluate the intra-examiner reproducibility of probing pocket depth (PPD) measurements with a four types of manual periodontal probes. Methods: Previously accepted by an Ethical Committee and after informed consent, 20 subjects without periodontal disease were selected if they presented at least 6 teeth per quadrant without antibiotic therapy in the last 8 months. One calibrated examiner (k>0.6), will assess PPD from all teeth at 6 sites/tooth with Williams (1, 2, 3, 5, 7, 8, 9 and 10 mm), Colorvue (3, 6, 9 and 12mm); PDT Sensor Probe 2M-12 (2, 4, 6, 8, 10 and 12mm), and UNC 15/23 (1 to 15mm) manual periodontal probes from the gingival margin to the bottom of the periodontal sulcus (rounded to the next 0.5mm). Initial (Baseline) and repeated measurements will performed by one trained examiner.

Interventions

Periodontal probing depth with four types of manual probes in healthy volunteers One trained examiner will measure PD in 20 patients to determine the intra-examiner reproducibility with four types of manual periodontal probes in two times measurements by each patient and each probe (Baseline and repeated measurement) as follows: FIRST DAY: PD on Patient 1 (Baseline), SECOND DAY: PD on Patient 2 (Baseline), THIRD DAY: PD on Patient 3 (Baseline), FOURTH DAY: PD on Patient 4 (Baseline), FIFTH DAY:

Periodontal probing depth with four types of manual probes in healthy volunteers One trained examiner will measure PD in 20 patients to determine the intra-examiner reproducibility with four types of manual periodontal probes in two times measurements by each patient and each probe (Baseline and repeated measurement) as follows: FIRST DAY: PD on Patient 1 (Baseline), SECOND DAY: PD on Patient 2 (Baseline), THIRD DAY: PD on Patient 3 (Baseline), FOURTH DAY: PD on Patient 4 (Baseline), FIFTH DAY: PD on Patient 5 (Baseline) and Patient 1 (repeated probing), SIXTH DAY: PD on Patient 6 (Baseline) and Patient 2 (repeated probing), SEVENTH DAY: PD on Patient 7 (Baseline) and Patient 3 (repeated probing), EIGHTH DAY: PD on Patient 8 (Baseline) and Patient 4 (repeated probing), the sequence will continue at the same manner until reach the patient number 20. PD is defined as the measurement in millimeters from the gingival margin to the bottom of the gingival sulcus. The study will use a Williams manual periodontal probe (1, 2, 3, 5, 7, 8, 9 and 10 mm Hu-Friedy), Colorvue periodontal probe (3, 6, 9 and 12mm Hu-Friedy); PDT Sensor Probe 2M-12 (2, 4, 6, 8, 10 and 12mm Pro-Dentec, Batesville AR), and UNC 15/23 manual probe (1 to 15mm Paradise Dental Technologies). The examiner will introduce each probe in the interior of the gingival sulcus and following the length of the tooth until resistance will be felt by the penetrating probe. Each patient will have six sites probed per tooth (mesial buccal, buccal, distal buccal, mesial lingual, lingual and distal lingual), excluding third molars. The PD measurements will do using the following criteria: all measurements will be round to the closest 0.5 mm (up or down), when the PD measurements are exactly between two marks on the probe the closest millimeter immediately above the mark will recorded. Each patient will have a minimum of six teeth per quadrant in order to be included in the study. The perfect squares formula will be used to random distribution of probes and areas to will be probed.

Sponsors

Roberto Antonio Andrade Acevedo
Lead SponsorIndividual

Study design

Allocation
Non-randomised trial
Intervention model
Single group
Primary purpose
Diagnosis
Masking
Open (masking not used)

Eligibility

Sex/Gender
All
Age
0 to No maximum
Healthy volunteers
Yes

Inclusion criteria

Healthy patients: No signs of periodontal destructive disease (loss of clinical attachment).

Exclusion criteria

Patients who have received treatments of fixed or partial prosthetics, individual crowns or orthodontia; surgical or non-surgical periodontal treatments in the last eight months; been taking antibiotics; or be pregnant

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026